Results 71 to 80 of about 98,569 (252)

Concurrent Atypical Hemolytic Uremic Syndrome and Autoimmune Hemolytic Anemia: a case report

open access: yesCaspian Journal of Pediatrics, 2018
Background: Atypical hemolytic uremic syndrome (aHUS) is a life-threatening and scarce disorder characterized by acute renal failure and disease, non-immune microangiopathic hemolytic anemia and thrombocytopenia, leading to end-stage renal failure or ...
Sayed Yousef Mojtahedi   +1 more
doaj  

Hemolytic Anemia in Cirrhosis: A Case of Spur-Cell Anemia

open access: yesAnnals of Internal Medicine: Clinical Cases
Anemia is a common complication of cirrhosis; therefore, its evaluation must be thorough and tailored to a patient's history. In this case, a 67-year-old woman with metabolic dysfunction–associated cirrhosis presented with transfusion-refractory ...
Blake H. Bentley   +2 more
doaj   +1 more source

The "erythrocyte-coating substance" of "auto-immune" hemolytic disease [PDF]

open access: yes, 1957
Thesis (M.A.)--Boston ...
Fudenberg, Hugh
core  

Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification. [PDF]

open access: yes, 2020
Since 2013, the International Union of Immunological Societies (IUIS) expert committee (EC) on Inborn Errors of Immunity (IEI) has published an updated phenotypic classification of IEI, which accompanies and complements their genotypic classification ...
Ailal, Fatima   +18 more
core  

The Prevalence of Peripheral Erythrophagocytosis in Pediatric Immune-Mediated Hemolytic Anemia

open access: yesHematology Reports
Background: Peripheral erythrophagocytosis appears to be a unique sign of acquired immune-mediated hemolytic anemia. It is said to be rare but its prevalence among patients with autoimmune hemolytic anemia has not been studied.
Anselm Chi-wai Lee
doaj   +1 more source

Hemolytic Anemia and Reactive Thrombocytosis Associated With Cefoperazone/Sulbactam

open access: yesFrontiers in Pharmacology, 2019
Background: Cefoperazone/sulbactam is a broad-spectrum antibacterial agent. Drug-induced immune hemolytic anemia is a rare but serious condition, and reactive thrombocytosis is caused by processes extrinsic to the megakaryocyte.
Ling Zhou, Jianan Bao, Jingjing Ma
doaj   +1 more source

DETECTION OF OCCULT GLOMERULAR DYSFUNCTION IN GLUCOSE SIX PHOSPHATE DEHYDROGENASE DEFICIENCY ANEMIA

open access: yesMediterranean Journal of Hematology and Infectious Diseases, 2016
Background:  Glucose six phosphate dehydrogenase deficiency (G6PD) anemia is associated with intravascular hemolysis. The freely filtered hemoglobin can damage the kidney. We aimed to assess gloumerular status in G6PD children.
Gehan Abdel Hakeem   +6 more
doaj   +1 more source

Babesiosis-induced warm autoimmune hemolytic anemia, from infection to hemolysis: a case report

open access: yesJournal of Medical Case Reports
Background Warm autoimmune hemolytic anemia is characterized by destruction of red blood cells mediated by autoantibodies, which can be triggered by various underlying factors including tick-borne infections. Babesia spp.
Jenna Davison   +6 more
doaj   +1 more source

Comorbidities in aging patients with sickle cell disease. [PDF]

open access: yes, 2018
Sickle cell disease (SCD) in general and sickle cell anemia in particular is a highly complex disorder both at the molecular and clinical levels. Although the molecular lesion is a single-point mutation, the sickle gene is pleiotropic in nature causing ...
Ballas, Samir K.
core   +2 more sources

Acute hemolysis in association with hepatitis B infection in a child with beta-thalassemia trait

open access: yesThe Turkish Journal of Pediatrics, 1994
Autoimmune hemolytic anemia may occur in the course of some viral diseases such as Coxsackie virus, cytomegalovirus, Epstein Barr virus, Influenza A, herpes simplex virus, and rarely hepatitis B virus infection.
A Gürgey, A Yüce, N Ozbek, N Koçak
doaj  

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